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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063290Generated: October 31, 2026

Ammonium Acetate → HCID 22278866, compound

https://huagongshe.com/reaction/1063290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Carbethoxy-3-ethyl-4-piperidoneHCID 22278851—
SolventMethanolHCID 887—
ProductHCID 22278866HCID 22278866—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ammonium acetate (33 g) was added to the stirred solution of 1-carbethoxy-3-ethyl-4-piperidinone (8.2 g, 41 mmol) in methanol (125 ml) and stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (2.5 g, 39 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 6 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish crude 4-amino-1-carbethoxy-3-ethylpiperidine, which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-9c8154a7bc0649b5bff92960bbbc5fae
Source noteuspto-grants-2005_11